Canonical Allele Identifier: PA2830415660
Gene: PLTP HGNC NCBI

Linked Data

ClinVar Variation Id: 1469132
ClinVar RCV Id: RCV001961425
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_872617.1:p.Thr175Ser
CA409195805
NM_182676.3:c.524C>G
CA409195809
NM_182676.3:c.523A>T